Regulation mechanism of melanin production by related-genes and UV.

相关基因和紫外线对黑色素生成的调控机制。

基本信息

  • 批准号:
    14570829
  • 负责人:
  • 金额:
    $ 1.92万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    2002
  • 资助国家:
    日本
  • 起止时间:
    2002 至 2003
  • 项目状态:
    已结题

项目摘要

Contents of pheomelanin and its precursor, 5-S-cysteinyldopa in culture media from agouti (C57BL/10JHir-A/A) melanocytes was increased by L-tyrosine compared with black (a/a ; CS7BL/10JHir) melanocytes. Moreover, pheomelanin content in the epidermis from 3.5-and 5.5-day-old A/A mice was much higher than a/a mice. The A gene was expressed in the A/A dermis of 0.5-, 3.5-and 5.5-day-old mice, but not in the a/a dermis as well as in the A/A and a/a epidermis. These results suggest that pheomelanin production in the epidermis from 3.5-and 5.5-day-old A/A mice is induced by the expression of the agouti gene in the dermis.The study using melanocyte culture system of newborn mice wild-type at the pink-eyed dilution (p) locus (black ; C57BL/10JHir) and from congenic mice mutant at that locus (C57BL/10JHir-p/p) showed that the proliferation of p/p melanoblasts/melanocytes was stimulated by L-tyrosine (Tyr), and that the differentiation of melanocytes was induced by L-Tyr as the age of the donor mice advanced, even though eumelanin and pheomelanin failed to accumulate in p/p melanocytes and were released from them at all ages of skin development.Moreover, the study using melanocyte culture system of newborn mice wild-type at the slaty (sit) locus (black ; C57BL/10THir) and from congenic mice mutant at that locus (C57BL/10JHir-slt/slt) or of newborn mice wild-type at extension (e) locus (black : C57BL/10JHir) and from congenic mice mutant at that locus (C57BL/10JHir-e/e) showed eumelanin synthesis was inhibited in slt/slt melanocytes, and that both eumelanin and pheomelanin were synthesized in epidermis and dermis and their synthesis increased in e/e epidermis and dermis as skin development proceeded.
L-酪氨酸能增加黑素细胞培养液中的褐黑素及其前体5-S-半胱氨酰多巴的含量。此外,3.5和5.5日龄A/A小鼠表皮中的褐黑素含量远高于a/a小鼠。A基因在0.5、3.5和5.5日龄小鼠的A/A真皮中表达,但在a/a真皮以及A/A和a/a表皮中不表达。这些结果表明,3.5和5.5日龄A/A小鼠表皮中的褐黑素产生是由真皮中agglutinase基因的表达诱导的。(黑色; C57 BL/10 JHir)和来自该位点突变的同类小鼠(C57 BL/10 JHir-p/p)显示p/p成黑素细胞/黑素细胞的增殖被L-酪氨酸(Tyr)刺激,并且随着供体小鼠年龄的增长,黑素细胞的分化被L-Tyr诱导,即使真黑素和褐黑素不能在p/p黑素细胞中积累并且在皮肤发育的所有年龄从它们释放。使用新生小鼠野生型黑素细胞培养系统在Slaty(sit)位点的研究(黑色; C57 BL/10 THir)和来自该基因座突变的同类小鼠(C57 BL/10 JHir-slt/slt)或新生小鼠在延伸(e)基因座处的野生型(黑色:C57 BL/10 JHir)和来自该位点突变的同类小鼠(C57 BL/10 JHir-e/e)显示在slt/slt黑素细胞中真黑素合成受到抑制,真黑素和褐黑素均在表皮和真皮中合成,且随着皮肤发育,它们在E/E表皮和真皮中的合成增加。

项目成果

期刊论文数量(160)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
S.Ito: "Structure and function of Neuromelanin"Academic/Plenum Publishers. 4 (2002)
S.Ito:“神经黑色素的结构和功能”学术/全会出版社。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
T.Hirobe: "Effects of genic substitution at the pink-eyed dilution locus on the proliferation and differentiation of mouse epidermal melanocytes in vivo and in vitro."J. Ex Zool.. 292. 351-366 (2002)
T.Hirobe:“红眼稀释基因座的基因替换对体内和体外小鼠表皮黑素细胞增殖和分化的影响”。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
T.Ye: "Ultrafast absorption and photothermal studies of decarboxytrichochrome C in Solution."Photochem.Photobiol.Sci.. 2. 821-823 (2003)
T.Ye:“溶液中脱羧毛色素 C 的超快吸收和光热研究。”Photochem.Photobiol.Sci.. 2. 821-823 (2003)
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Y.Yukitake: "Synthesis and selective in vitro anti-melanoma effect of enantiomeric alpha-methyl- and alpha-ethyl-4-S-cysteaminylphenol."Melanoma Res. 13. 603-609 (2003)
Y.Yukitake:“对映体α-甲基-和α-乙基-4-S-半胱氨基苯酚的合成和选择性体外抗黑色素瘤作用。”黑色素瘤研究。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
S.Ito: "Quantitative analysis od eumelanin and pheomelanin in humans, mice, and other animals : a comparative review."Pigment Cell Res. 16. 523-531 (2003)
S.Ito:“人类、小鼠和其他动物中真黑素和褐黑素的定量分析:比较综述。”色素细胞研究。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
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ITO Shosuke其他文献

ITO Shosuke的其他文献

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{{ truncateString('ITO Shosuke', 18)}}的其他基金

Elucidation of ultraviolet radiation-induced physiological degradation pathway of eumelanin and pheomelanin and its physiological significance
紫外辐射诱导的真黑素和褐黑素生理降解途径及其生理意义的阐明
  • 批准号:
    26461705
  • 财政年份:
    2014
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Elucidation of ultraviolet radiation-induced physiological degradation pathway of eumelanin and pheomelanin
阐明紫外线辐射诱导的真黑素和褐黑素的生理降解途径
  • 批准号:
    23591659
  • 财政年份:
    2011
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Control mechanism of melanogenesis by pigmentation-related genes and ultraviolet radiation
色素沉着相关基因和紫外线对黑色素生成的控制机制
  • 批准号:
    20591357
  • 财政年份:
    2008
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Mechanism of regulation of melanin synthesis by coat color genes and ultraviolet radiation in mice and human
毛色基因和紫外线调节小鼠和人类黑色素合成的机制
  • 批准号:
    18591262
  • 财政年份:
    2006
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Genetic and non-genetic regulation mechanism of melanin production in the mammal
哺乳动物黑色素产生的遗传和非遗传调控机制
  • 批准号:
    12670844
  • 财政年份:
    2000
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
ANALYSIS OF REGULATIVE FUNCTION OF MELANIN-RELATED GENE EXPRESSION BY BIOCHEMICALAND CELLULAR BIOLOGICAL METHODS
生物化学和细胞生物学方法分析黑色素相关基因表达的调控功能
  • 批准号:
    10670812
  • 财政年份:
    1998
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Functions of Melanogenesis-Related Genes by Chemical and Biochemical Methods
通过化学和生化方法研究黑素生成相关基因的功能
  • 批准号:
    07670971
  • 财政年份:
    1995
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Biochemical Markers of Melanoma Utilizing Melanin Formation
利用黑色素形成的黑色素瘤的生化标志物
  • 批准号:
    02670487
  • 财政年份:
    1990
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)
Biosynthesis of Eumelanin in Melanoma and Biochemical Markers of Melanoma
黑色素瘤中真黑素的生物合成及黑色素瘤的生化标志物
  • 批准号:
    63570484
  • 财政年份:
    1988
  • 资助金额:
    $ 1.92万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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